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长链非编码RNA MAFG-AS1作为肝细胞癌的潜在生物标志物:与肿瘤特征、标志物、肝功能及生存情况的关联

Long Non-Coding RNA MAFG-AS1 as a Potential Biomarker for Hepatocellular Carcinoma: Linkage with Tumor Features, Markers, Liver Functions, and Survival Profile.

作者信息

Tian Yuanyuan, Wang Jiao, Tian Ge, Li Bing, Chen Moli, Sun Xiaoning

机构信息

Department of Gastroenterology, Hainan General Hospital/Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.

Department of Infectious Diseases, Hainan General Hospital/Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.

出版信息

Front Surg. 2022 May 17;9:848831. doi: 10.3389/fsurg.2022.848831. eCollection 2022.

DOI:10.3389/fsurg.2022.848831
PMID:36034393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9406288/
Abstract

PURPOSE

Long non-coding RNAs musculoaponeurotic fibrosarcoma oncogene family, protein G antisense 1 (lnc-MAFG-AS1) regulates hepatocellular carcinoma (HCC) progression and treatment resistance in multiple ways, while its engagement in HCC clinical management remains obscure. The current study aims to explore the relationship of lnc-MAFG-AS1 with tumor features, liver function indexes, tumor markers, and prognosis in HCC patients.

METHODS

One hundred and fifty-two surgical HCC patients who underwent tumor resection were retrospectively analyzed. Their tumor and adjacent tissues were acquired and then proposed to reverse transcription-quantitative polymerase chain reaction to detect lnc-MAFG-AS1 expression.

RESULTS

Lnc-MAFG-AS1 expression was increased in HCC tumor tissue than in adjacent tissue [median (interquartile range): 2.730 (1.685-4.198) vs. 0.990 (0.703-1.468), < 0.001], with a high area under the curve [0.889, 95% confidence interval (CI): 0.854-0.924] to distinguish them via receiver operating characteristic curve analysis. Tumor lnc-MAFG-AS1 was linked with multifocal nodules (< 0.001), increased Barcelona Clinic Liver Cancer (BCLC) stage (= 0.018), and elevated China Liver Cancer (CNLC) stage (= 0.008), which also correlated with an abnormal alpha-fetoprotein (AFP) level (= 0.004), However, lnc-MAFG-AS1 was not linked with other disease conditions, tumor properties, liver function indexes, or tumor markers (all s> 0.05). In addition, patients with a high expression of lnc-MAFG-AS1 exhibited worse overall survival than those with a low expression of lnc-MAFG-AS1 [median (95% CI): 34.0 (24.5-43.5) vs. 48.0 (41.5-54.5) months] (= 0.011), which was further validated by univariate Cox's analysis [hazard ratio (HR) = 1.827, = 0.013] and multivariate Cox's analysis (HR = 1.697, = 0.040).

CONCLUSION

Lnc-MAFG-AS1 relates to multifocal nodules, increased BCLC stage, elevated CNLC stage, and abnormal AFP level and predicts pejorative prognosis in HCC patients.

摘要

目的

长链非编码RNA肌肉腱膜纤维肉瘤癌基因家族蛋白G反义1(lnc-MAFG-AS1)通过多种方式调节肝细胞癌(HCC)的进展和治疗耐药性,但其在HCC临床管理中的作用仍不清楚。本研究旨在探讨lnc-MAFG-AS1与HCC患者肿瘤特征、肝功能指标、肿瘤标志物及预后的关系。

方法

回顾性分析152例行肿瘤切除术的手术HCC患者。获取他们的肿瘤组织和癌旁组织,然后进行逆转录定量聚合酶链反应以检测lnc-MAFG-AS1的表达。

结果

lnc-MAFG-AS1在HCC肿瘤组织中的表达高于癌旁组织[中位数(四分位间距):2.730(1.685-4.198)对0.990(0.703-1.468),<0.001],通过受试者工作特征曲线分析,其曲线下面积较高[0.889,95%置信区间(CI):0.854-0.924],可用于区分两者。肿瘤lnc-MAFG-AS1与多灶性结节相关(<0.001)、巴塞罗那临床肝癌(BCLC)分期增加(=0.018)和中国肝癌(CNLC)分期升高(=0.008),这也与甲胎蛋白(AFP)水平异常相关(=0.004)。然而,lnc-MAFG-AS1与其他疾病情况、肿瘤特性、肝功能指标或肿瘤标志物均无关联(所有P>0.05)。此外,lnc-MAFG-AS1高表达的患者总生存期比lnc-MAFG-AS1低表达的患者更差[中位数(95%CI):34.0(24.5-43.5)对48.0(41.5-54.5)个月](=0.011),单因素Cox分析[风险比(HR)=1.827,=0.013]和多因素Cox分析(HR=1.697,=0.040)进一步验证了这一结果。

结论

lnc-MAFG-AS1与多灶性结节、BCLC分期增加、CNLC分期升高及AFP水平异常相关,并可预测HCC患者的不良预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/43269f034db5/fsurg-09-848831-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/d888cb4ab2bb/fsurg-09-848831-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/eb74198bb123/fsurg-09-848831-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/98ecf3d9f541/fsurg-09-848831-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/43269f034db5/fsurg-09-848831-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/d888cb4ab2bb/fsurg-09-848831-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/eb74198bb123/fsurg-09-848831-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/98ecf3d9f541/fsurg-09-848831-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c4/9406288/43269f034db5/fsurg-09-848831-g004.jpg

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